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Glycan Syntheses |
JCGG ID |
JCGG-RAC0001756 | |||||||
Submitter |
The Noguchi Institute | |||||||
Reaction ID |
R-0000-001756
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Regist Date |
2012/06/21 17:52:37 | |||||||
| REACTANT | ||||||||
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Mol |
1.25 mmol | |||||||
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Mol |
1.03 mmol | |||||||
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Reactant Type |
IDCP | |||||||
Mol |
1.65 mmol | |||||||
| PRODUCT | ||||||||
MOLECULE ID |
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Yield |
63% | |||||||
| REACTION DETAIL | ||||||||
Reaction Time |
10 hours | |||||||
Reaction Temp |
room temp | |||||||
Solvent |
dry Et2O/CH2Cl2 = 4/1 | |||||||
Comment |
MS 4A was included in the solvent. | |||||||
| The reaction was conducted in dark condition. | ||||||||
| COMMENT | ||||||||
| Keywords: oligosaccharide synthesis, n-pentenyl glycosides, NPG Coupling, IDCP | ||||||||
| REFERENCE | ||||||||
Reference Id |
REF-0000-000196 | |||||||
Source |
PREPARATIVE CARBOHYDRATE CHEMISTRY | |||||||
Reference Id |
REF-0000-000197 | |||||||
Source |
ISBN 0-8247-9802-3 | |||||||
Reference Id |
REF-0000-000239 | |||||||
Source |
Carbohydr. Res. 216:323 (1991) | |||||||
©2008-2013 Research Center for Medical Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST)
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